SE-ATLAS

Proximal spinal muscular atrophy type 2 Cyprus facial-neuromusculoskeletal syndrome Infectious, fungal or parasitic myopathy Proximal spinal muscular atrophy type 4 Proximal spinal muscular atrophy type 3 Primary lateral sclerosis Idiopathic camptocormia Lower motor neuron syndrome with late-adult onset Spinal muscular atrophy associated with central nervous system anomaly Muscular dystrophy-white matter spongiosis syndrome Autosomal dominant childhood-onset proximal spinal muscular atrophy Autosomal dominant adult-onset proximal spinal muscular atrophy Amyotrophic lateral sclerosis type 4 Madras motor neuron disease Vacuolar myopathy with sarcoplasmic reticulum protein aggregates Autosomal dominant distal hereditary motor neuropathy Amyotrophic lateral sclerosis Muscular channelopathy Autosomal recessive distal hereditary motor neuropathy Isaacs syndrome Morvan syndrome Proximal spinal muscular atrophy type 1 Skeletal muscle disease Hypokalemic periodic paralysis Muscular dystrophy Hyperkalemic periodic paralysis Paramyotonia congenita of Von Eulenburg Juvenile amyotrophic lateral sclerosis Genetic skeletal muscle disease Idiopathic inflammatory myopathy Acquired skeletal muscle disease Malignant hyperthermia of anesthesia Neuromuscular junction disease Acquired neuromuscular junction disease Tel Hashomer camptodactyly syndrome Lambert-Eaton myasthenic syndrome Genetic neuromuscular junction disease Non-dystrophic myopathy X-linked distal spinal muscular atrophy type 3 Motor neuron disease Myotonia fluctuans Acquired motor neuron disease Genetic motor neuron disease Myotonie sensible à l'acétazolamide Myotonie permanente Syndrome scapulo-péronier neurogénique type Kaeser Myasthénie auto-immune de l'adulte Amyotrophie spinale proximale autosomique dominante Myasthénie auto-immune Syndrome myasthénique congénital Syndrome de déficience intellectuelle-retard de développement-contractures Paralysie périodique génétique Syndrome d'Andersen-Tawil Myofasciite à macrophages Poliomyélite Maladie neuromusculaire Myasthénie auto-immune juvénile Myopathie distale Sclérose latérale primitive juvénile Amyotrophie spinale infantile liée à l'X Myasthénie auto-immune transitoire du nouveau-né Paralysie spastique infantile ascendante héréditaire Amyotrophie bulbospinale Myotonie aggravée par le potassium Syndrome myotonique Myotonie congénitale de Thomsen et Becker Amyotrophie spinale proximale Amyotrophie bulbospinale de l'enfant Paralysie périodique Tumeur musculaire Amyotrophie bulbospinale de l'adulte Syndrome post-poliomyélite Rippling muscle disease avec myasthenia gravis Amyotrophie spinale généralisée Amyotrophie monomélique